Canonical Allele Identifier: CA343759
Gene: TERC HGNC NCBI

Linked Data

ClinVar Variation Id: 39287
ClinVar RCV Id: RCV000032567
dbSNP Id: rs199422259
MyVariant Identifiers: chr3:g.169482815_169482821del (hg19) chr3:g.169765027_169765033del (hg38)
PubMed: PMID:20301779
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169765029_169765035del , CM000665.2:g.169765029_169765035del GRCh38
NC_000003.11:g.169482817_169482823del , CM000665.1:g.169482817_169482823del GRCh37
NC_000003.10:g.170965511_170965517del NCBI36
NG_016363.1:g.5028_5034del , LRG_347:g.5028_5034del

Transcript Alleles

HGVS Amino-acid change
NR_001566.1:n.28_34del , LRG_347t1:n.28_34del
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